Publication: Revisiting TOP2B-related phenotypes: three new cases and literature review
dc.contributor.coauthor | Kalayci, Tugba | |
dc.contributor.department | KUH (Koç University Hospital) | |
dc.contributor.department | Graduate School of Health Sciences | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Çepni, Ece | |
dc.contributor.kuauthor | Börklü Yücel, Esra | |
dc.contributor.kuauthor | Avcı, Şahin | |
dc.contributor.kuauthor | Eraslan, Serpil | |
dc.contributor.kuauthor | Kayserili, Hülya | |
dc.contributor.schoolcollegeinstitute | GRADUATE SCHOOL OF HEALTH SCIENCES | |
dc.contributor.schoolcollegeinstitute | KUH (KOÇ UNIVERSITY HOSPITAL) | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2025-01-19T10:29:49Z | |
dc.date.issued | 2023 | |
dc.description.abstract | DNA Topoisomerase II beta (TOP2B) acts on DNA topology during transcription and has a critical role in neural development. Heterozygous pathogenic changes in its encoding gene, TOP2B (MIM *126431), has been linked with three overlapping phenotypes characterized by immunodeficiency, acral and urogenital anomalies: Hoffman, BILU and Ablepharon-macrostomia-like syndrome. We herein report on a mother and two sons with distinct TOP2B-phenotype. Two males reported further delineated genital phenotype of males and all reported patients were reviewed for genotypephenotype correlation. We believe the patients reported herein along with the previously defined 11 represent a phenotypic spectrum from mild-to-severe immunological, acral and urogenital involvement, for which we propose the acronym "TOP2B-related Immunodeficiency and Congenital Anomalies Spectrum (TICAS)". | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 2 | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.sponsorship | TUBITAK, grant number 112S398 (E-RARE network CRANIRARE2) to HK. | |
dc.description.volume | 104 | |
dc.identifier.doi | 10.1111/cge.14341 | |
dc.identifier.eissn | 1399-0004 | |
dc.identifier.issn | 0009-9163 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-85153229201 | |
dc.identifier.uri | https://doi.org/10.1111/cge.14341 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/25954 | |
dc.identifier.wos | 971729100001 | |
dc.keywords | B-cell immunodeficiency | |
dc.keywords | BILU syndrome | |
dc.keywords | Hoffman syndrome | |
dc.keywords | TOP2B gene | |
dc.language.iso | eng | |
dc.publisher | Wiley | |
dc.relation.grantno | TUBITAK [112S398] | |
dc.relation.ispartof | Clinical Genetics | |
dc.subject | Genetics and heredity | |
dc.title | Revisiting TOP2B-related phenotypes: three new cases and literature review | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Çepni, Ece | |
local.contributor.kuauthor | Börklü Yücel, Esra | |
local.contributor.kuauthor | Avcı, Şahin | |
local.contributor.kuauthor | Eraslan, Serpil | |
local.contributor.kuauthor | Kayserili, Hülya | |
local.publication.orgunit1 | GRADUATE SCHOOL OF HEALTH SCIENCES | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit1 | KUH (KOÇ UNIVERSITY HOSPITAL) | |
local.publication.orgunit2 | KUH (Koç University Hospital) | |
local.publication.orgunit2 | School of Medicine | |
local.publication.orgunit2 | Graduate School of Health Sciences | |
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